European MDR 2017/745 Transition Timelines and Strategies

Download our white paper on the European MDR Transition Timelines and Strategies

Medical device companies selling in Europe are preparing to transition to the new Medical Device Regulation (MDR 2017/745). The transition deadline seems distant, but there are a lot of factors to consider when coordinating and planning the transition strategy for your company.

In this white paper, we provide an in-depth discussion of the transition process and how to choose the best transition timeline for your company. You will learn:

  • What to do and when to be in line with the MDR
  • How notified body recertification could affect your transition
  • When to transition to ISO 13485:2016
  • Four possible transition timelines
  • Detailed transition steps

Learn all this and much more in this 10-page white paper.

About the Author:

Ronald Boumans, MsC is Senior Regulatory Consultant at Emergo's office in The Hague. He previously served as Inspector of Medical Technology at the Dutch Healthcare Inspectorate (IGZ), and his areas of expertise include European medical device legislation, Competent Authority supervision, and CE Marking requirements.